PAH patients in England denied new treatment

7 July 2018

Actelion, which is now part of US healthcare giant Johnson & Johnson (NYCE: JNJ), has announced that Uptravi (selexipag) will not be funded on the National Health Service (NHS) in England, meaning patients with life-limiting disease, pulmonary arterial hypertension (PAH), are forced to continue to wait for access.

Actelion Pharmaceuticals UK & Ireland, which is now part of US healthcare giant Johnson & Johnson (NYCE: JNJ), today announced that an NHS England ruling means patients in England who have a life-limiting condition must continue to wait for access to a new twice daily tablet for pulmary arterial hypertension (PAH).

Uptravi was approved by European and US regulators in 2016 and 2015, respectively, prior to the $30 billion acquisition of Swiss biotech firm Actelion by J&J.

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